Cyclopropanecarboxylic acid → Cyclopropanecarboxylic acid anhydride
Reaction equation
[CH:1]1([C:4]([OH:6])=[O:5])[CH2:3][CH2:2]1.[CH:7]1([C:10](Cl)=[O:11])[CH2:9][CH2:8]1>>[CH:1]1([C:4]([O:6][C:10]([CH:7]2[CH2:9][CH2:8]2)=[O:11])=[O:5])[CH2:3][CH2:2]1Participants
3
Procedure
This was prepared from cyclopropanecarboxylic acid (Aldrich) and cyclopropanecarboxylic acid chloride (Aldrich) by the method given (Example IV) for the preparation of the cyclobutyl analogue and purified by vacuum distillation; bp 95°-100° C. at 6 torr (lit.: Castro and Dormoy, Bull. Soc. Chem. Fr. 8, 3034 (1971) bp 102°-104° C. at 8 torr); IR anhydride C=O stretch absorptions at 5.53 and 5.74μ.
Workup
- distillationpurified by vacuum distillation
Sources & evidence
- ORD record
- ord-a690a1f727504d85a62688187e3542e8
- Source dataset
- uspto-grants-1979_02
- Patent number
- US04141897
Reaction notes
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